Arrow recalls Hands-Off Multi-Lumen Central Venous Catheters with Blue FlexTip due to potential packaging compromise affecting sterility. Affected models include HO-14702 and others listed. Consumers should check packaging seals.
The packaging may not be sealed. If the packaging is compromised in this manner, the sterility of the product cannot be guaranteed.
Arrow is recalling Hands-Off Multi-Lumen Central Venous Catheters with Blue FlexTip because the packaging might not be sealed properly. This could mean the catheter isn't sterile when used, which is dangerous for medical procedures.
If the packaging isn't sealed, the catheter might not be sterile. This could lead to infections or other complications during medical procedures since the catheter is inserted directly into the bloodstream.
Healthcare professionals who use these catheters for medical procedures are most at risk. Patients receiving these catheters through medical facilities may also be affected.
Check for the model numbers HO-14702, 14F15F0156, 14F15H0228, 14F15K0746, 14F16B0085, 14F16D0424, 14F16F0700, or 14F16G0471 on the packaging. These catheters are designed to work with Arrow One-Piece Percutaneous Sheath Introducer Systems.
Look for signs that the packaging is not sealed properly, which could compromise sterility.
The packaging may not be sealed, which could mean the catheter isn't sterile when used. This poses a risk of infection during medical procedures.
The affected models include HO-14702, 14F15F0156, 14F15H0228, 14F15K0746, 14F16B0085, 14F16D0424, 14F16F0700, and 14F16G0471.
The recall does not require stopping use immediately. However, you should check if the packaging is sealed properly before use.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-2818-2018 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-2818-2018 from Arrow. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
